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Health Services, GeriatricSCOPENCT01672177

Self Care for Older Persons in Singapore: An Intervention Study

A study testing Chronic disease self-management training in people with Health Services, Geriatric, run by National University of Singapore at 12 sites in Singapore.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The main aim of the project is to evaluate a self-care intervention program aimed at enhancing the ability of mildly disabled and healthy older persons in Singapore to manage their health. Read more about this study

Who is it for?
Ages 55 years and olderHealthy volunteers can take part
Conditions the study is for
Health Services, Geriatric
What is being tested?
Chronic disease self-management training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
400 participants
Where
12 sitesSingapore
Study dates
Aug 2011to Oct 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 55 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age 55 and above
  • Age 21 or above for CHTs
  • No cognitive impairment as justified by AMT
  • No Activities of Daily Living (ADL)Limitations preventing them from coming to questionnaire interviews, health screenings, and/or weekly health trainings.
  • Not severely ill ; not on dialysis, chemotherapy or psychiatric medication

Who cannot join

  • Below 55 years of age
  • Cognitively impaired
  • Severely depressed
  • With ADLs preventing them from coming to questionnaire interviews, health screenings, and/or weekly health trainings.
  • Severely ill ; on dialysis, chemotherapy or psychiatric medication
  • Those who refused to have their biomarkers taken (applies to both intervention and non-intervention group)

Trial locations and contacts

12 sites in 1 country.

12 sites in 1 country

Singapore12 sites
  • Redhill SilverACE

    Singapore, 150071

  • Moral Seniors Activity Centre (Redhill)

    Singapore, 150089

  • Moral Neighbourhood Link Bukit Merah View/Tanjong Pagar FSC

    Singapore, 150118

  • Kreta Ayer Seniors Activity Centre (Chin Swee)

    Singapore, 160051

  • Sarah Seniors Activity Centre

    Singapore, 160105

  • Kreta Ayer Senior Activity Centre (Jalan Kukoh)

    Singapore, 162008

  • AWWA Seniors Activity Centre

    Singapore, 560123

  • Ang Mo Kio Family Services Centre

    Singapore, 560230

  • Community Care Network Senior Activity Centre @Teck Ghee 420

    Singapore, 560420

  • Care Corner Toa Payoh

    Singapore

  • Lion Befrienders/TOUCH

    Singapore

  • Moral Neighbourhood Link Telok Blangah

    Singapore

Other trials in Singapore

About this study

The main aim of the project is to evaluate a self-care intervention program aimed at enhancing the ability of mildly disabled and healthy older persons in Singapore to manage their health.

A secondary aim of the study is to evaluate the effectiveness of training community health workers located within Senior Activity Centres in Singapore to support the self-care capacity development amongst older persons in the locale.

Read the detailed description

Singapore is facing a rapidly ageing population due to its changing demographics. One of the biggest challenges associated with older adults is providing them with adequate and sustainable health care. There are four main barriers that make it challenging to do so in this segment of the population: (1) Lack of knowledge of simple coping mechanisms and self care; (2) inadequate access to care and healthcare; (3) social, economic, and political exclusion; and (4) declining family support and strains on state services.

This proposal, is to conduct a randomized controlled trial that tests the impact of a state-of-the-art self care training program focused on teaching older adults how to manage their health and if present, their diabetes, hypertension or chronic obstructive pulmonary disease. The training focuses on health promotion, disease prevention, health seeking behavior, chronic disease management and empowerment. The study period is 18 months with measurements taken at baseline, 8 months and 18 months. Major events (stroke, myocardial infarction, end-stage renal disease, hospitalization, deaths) during the study will also be recorded. A questionnaire assessing functional status (IADL), quality of life (EQ5D), knowledge and attitude about health care, health seeking behavior, and health status (CIRS-G) will be used. Anthropometric measures will also be taken to better understand certain aspects related to the health and physical status of the participants as well as biomarkers such as the levels of glycosylated hemoglobin (HbA1c), cholesterol (total HDL), triglycerides, blood pressure and peak expiratory flow.

The main goal of the study is to improve each individual score and to measure improvement in overall quality of life and mental well-being. The total sample size for this pilot study is 400 older persons (above 55 years of age) randomly sampled from Tiong Bahru/Bukit Merah and Ang Mo Kio. The health care training will be based in Senior Activity Centres (SACs) located in HDB blocks. The investigators will select 12 SACs and randomly assign 6 SACs to the intervention group and 6 SACs to the control group. All twelve groups will receive a baseline assessment of physical and mental health status and a follow-up at 8 and 18 months. Two community health trainers (CHT) will be assigned to each of the intervention groups. These CHTs will have been trained by personnel at the Tsao Foundation to conduct the training protocol and collect data from participants. The intervention group will then receive the health care training once a week for 2 hours over a period of seven-eight months (56 hours total). The content of training materials focuses on health promotion, disease prevention, health seeking behavior, chronic disease management, and anti-stigmatization. In addition, each participant, regardless of randomization, will be given an event diary at baseline. The diary will be used to record any health related events that occur during the course of the study. Such events would include visits to GPs or traditional medicine practitioners, purchasing medications, hospitalization, etc.

The investigators hypothesize that the study will demonstrate the following: 1) Improve chronic disease outcomes for individuals presenting with these diseases: hypertension (20% decrease in systolic blood pressure), diabetes (1% decrease in HBA1C levels), and COPD (10% increase in peak expiratory flow) over the 18-month study period. 2) Improve quality of life of participants and their caregivers. 3) Improve knowledge, behaviours and attitudes towards health care utilization. 4) Develop a community health worker capacity in low-income settings. 5) Reduce the number of hospitalizations, outpatient and emergency visits in the intervention group.

This pilot study will also allow the investigators to test their methods for recruitment, training, and evaluation of the self-care training program. If successful, this study will provide evidence that older adults in the intervention group can more effectively manage their own health care and avert or delay the onset of disability compared to older adults in the control group. One of the long term goals is to replicate this study in Cambodia, India, Indonesia, and Vietnam. The investigators have identified academic and practice partners in each of these countries who have expressed an interest in the project and donors are awaiting the results from this pilot study before funding the regional components.

Being tested
Chronic disease self-management training
Keywords
Geriatrics, Aged, Aging, Chronic disease, Self management
Medical subject headings
Chronic Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Chronic disease self-management trainingBehavioural

    Those in the intervention group will receive two hour long weekly training sessions for seven-eight months (a total of 56 hours of training).

Study groups in NCT01672177
Study groupRoleWhat they receive
ControlNo interventionIndividuals in the control group will not receive any training.
InterventionExperimentalIndividuals in the intervention group will receive two hour long weekly training sessions for seven to eight months. The content of the training focuses on health promotion, health seeking behaviours and chronic disease management.
Receives: Behavioral: Chronic disease self-management training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Clinical Measures

    The primary outcome measure is a composite of the change in the following measures: 1)Systolic BP; 2)HbA1C; and 3)normalized peak flow. The null hypothesis is that there is no difference between intervention and control in any of the measures.

    Measured: 18 months

Secondary outcomes (3)
  1. Improved Quality of Life

    Improve quality of life of participants and their caregivers using a validated measure (EQ-5D).

    Measured: 18 months

  2. Community Health Trainer

    Develop a community health trainer capacity in low-income settings as assessed by numbers of individuals who successfully complete the health trainer education.

    Measured: 18 months

  3. Healthcare Utilization

    Reduce the number of hospitalizations, outpatient and emergency visits in the intervention group vs control.

    Measured: 18 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2012 (estimated)
  2. Study startAug 2011
  3. Primary completionOct 2014
  4. Study completionOct 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01672177
Sponsor's protocol ID
MOE2010-T2-2-107
Acronym
SCOPE
Status last verified
Apr 2015
First submitted
8 Aug 2012
Last updated
16 Apr 2015
Results posted
No
Data monitoring committee
No

Publications

  • Ng TKS, Wee HN, Ching J, Kovalik JP, Chan AW, Matchar DB. Plasma Acylcarnitines as Metabolic Signatures of Declining Health-Related Quality of Life Measure in Community-Dwelling Older Adults: A Combined Cross-sectional and Longitudinal Pilot Study. J Gerontol A Biol Sci Med Sci. 2024 Mar 1;79(3):glac114. doi: 10.1093/gerona/glac114.

    PubMed 35605263
  • Ng TKS, Matchar DB, Sultana R, Chan A. Effects of Self-Care for Older PErsons (SCOPE) on Functional and Physiological Measures: A Cluster Randomized Controlled Trial. J Clin Med. 2020 Mar 24;9(3):885. doi: 10.3390/jcm9030885.

    PubMed 32213860
  • Chan A, Matchar DB, Tsao MA, Harding S, Chiu CT, Tay B, Raman P, Pietryla Z, Klein MK, Haldane VE. Self-Care for Older People (SCOPE): a cluster randomized controlled trial of self-care training and health outcomes in low-income elderly in Singapore. Contemp Clin Trials. 2015 Mar;41:313-24. doi: 10.1016/j.cct.2015.01.001. Epub 2015 Jan 10.

    PubMed 25583272

Questions about this trial

What is this clinical trial studying?

A study testing Chronic disease self-management training in people with Health Services, Geriatric, run by National University of Singapore at 12 sites in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Apr 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 12 sites in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinical Measures (time frame: 18 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01672177, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2015; AzTrials last refreshed its copy on 6 Nov 2026.

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